69492-91-7

Basic information

• Product Name: 2-IODO-4-METHYL-6-NITROPHENOL
• Synonyms: 2-IODO-4-METHYL-6-NITROPHENOL
• CAS NO: 69492-91-7
• Molecular Formula: C₇H₆INO₃
• Molecular Weight: 279.03
• Mol File: 69492-91-7.mol

Chemical Properties

• Melting Point: 82-84°C
• Boiling Point: 254.4°C at 760 mmHg
• Flash Point: 107.6°C
• Appearance: /
• Density: 2.021g/cm³
• Vapor Pressure: 0.0108mmHg at 25°C
• Refractive Index: 1.684
• PKA: 5.79±0.38(Predicted)
• CAS DataBase Reference: 2-IODO-4-METHYL-6-NITROPHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-IODO-4-METHYL-6-NITROPHENOL(69492-91-7)
• EPA Substance Registry System: 2-IODO-4-METHYL-6-NITROPHENOL(69492-91-7)

Safety Data

• Hazard Codes: Xi
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 69492-91-7(Hazardous Substances Data)

Usage

Uses

Used in Chemical Synthesis:
2-IODO-4-METHYL-6-NITROPHENOL is used as a reagent or intermediate in various chemical reactions due to its high reactivity. Its presence of iodine, sulfur, and nitro groups makes it a valuable component in the synthesis of complex organic compounds.
Used in Laboratory Research:
In laboratory settings, 2-IODO-4-METHYL-6-NITROPHENOL is utilized for its unique properties in conducting experiments and studying chemical reactions. Its solubility in organic solvents and reactivity make it a useful tool for researchers in the field of organic chemistry.
Used in Pharmaceutical Industry:
2-IODO-4-METHYL-6-NITROPHENOL is used as a starting material or intermediate in the synthesis of pharmaceutical compounds. Its reactive nature allows for the creation of new drug molecules with potential therapeutic applications.
Used in Dye and Pigment Industry:
Due to its chemical structure, 2-IODO-4-METHYL-6-NITROPHENOL can be used in the production of dyes and pigments. Its ability to form various chemical compounds makes it a versatile component in the development of colorants for different applications.
Used in Environmental Analysis:
2-IODO-4-METHYL-6-NITROPHENOL can be employed as a reagent in environmental analysis, particularly in the detection and measurement of certain pollutants or contaminants. Its reactivity allows for specific chemical reactions that can be utilized in analytical processes.

InChI:InChI=1/C7H6INO3/c1-4-2-5(8)7(10)6(3-4)9(11)12/h2-3,10H,1H3

Upstream product

• 119-33-5 4-methyl-2-nitrophenol 
• 7664-41-7 ammonia 
• 7553-56-2 iodine 
• 106-44-5 p-cresol 

Downstream Products

• 1272662-49-3 2-((furan-2-ylmethyl)(2-iodo-4-methyl-6-nitrophenyl)amino)-N-(4-methoxybenzyl)propanamide 
• 1372134-63-8 2-(cyclopropyl(2-iodo-4-methyl-6-nitrophenyl)amino)-N-(4-methoxybenzyl)butanamide 
• 1372134-70-7 N-(4-methoxybenzyl)-2-(6-methyl-8-nitroquinolin-1(4H)-yl)butanamide 

Relevant articles and documents

Synthesis of hydrazone derivatives of benzofuran and their antibacterial and antifungal activity

A series of benzofuran hydrazones 6a–6n were synthesized from benzofuran aldehyde and substituted aromatic hydrazides 5a–5n. Structures of all compounds were confimed by IR, 1H and 13C NMR, and Mass spectral data. These compounds wer

Influence de la complexation sur la reactivite de nitrates d'halogenes

Iodine nitrate or bromine nitrate in acetonitrile or in chloroform react with a variety of phenolic substrates to form both halogenated and nitrated products.In the presence of strong complexing agents of halonium ions, no reacting occurs, while in the presence of pyridine or triethylamine, only halogenated phenols exhibiting a strong ortho-directing effect of the phenolic function are produced. Keywords: phenols, iodine nitrate, bromine nitrate, halogenation, nitration.

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The reaction of phenols with benzyltrimethylammonium dichloroiodate(1-) in dichloromethane-methanol in the presence of CaCO3 or NaHCO3 for several hours at room temperature gave iodophenols in good yields.